HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727953Generated: October 30, 2026
Dodecanoyl chloride → HCID 15728721, compound
https://huagongshe.com/reaction/727953
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dodecanoyl chloride | HCID 8166 | — |
| Reactant | 5-(Trimethylsilyl)furan-3-carbaldehyde | HCID 15663251 | — |
| Reactant | HCID 15728720 | HCID 15728720 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 15728721 | HCID 15728721 | — |
Reaction Steps
n-Butyl lithium (a 1.6M solution in hexane; 0.74 ml, 1.18 mmol) was added to a solution of 2-methoxyethoxy-methyl tributylstannylmethyl ether (481.6 mg, 1.18 mmol) in tetrahydrofuran (5 ml) at -78° under argon. After 10 minutes, a solution of 5-trimethylsilyl-3-furaldehyde (198 mg, 1.18 mmol) was added, followed by lauroyl chloride (0.26 ml, 1.18 mmol) after 20 minutes. Stirring was continued at room temperature for 48 hours and the mixture was quenched with water. Extraction (ether) and evaporation of the dried (magnesium sulphate) extracts gave an oil, which was flash chromatographed on silica using 20% ethyl ether/petroleum ether. Fractions with Rf of about 0.27 (30% ethyl ether/petroleum ether) on evaporation afforded the title ester as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05045564 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-637386894fa24973a3190f996b91507c |
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| Source note | uspto-grants-1991_09 |
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